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Targeting Cell Entry of Enveloped Viruses as an Antiviral Strategy

The entry of enveloped viruses into their host cells involves several successive steps, each one being amenable to therapeutic intervention. Entry inhibitors act by targeting viral and/or cellular components, through either the inhibition of protein-protein interactions within the viral envelope pro...

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Detalles Bibliográficos
Autores principales: Teissier, Elodie, Penin, François, Pécheur, Eve-Isabelle
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6259279/
https://www.ncbi.nlm.nih.gov/pubmed/21193846
http://dx.doi.org/10.3390/molecules16010221
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author Teissier, Elodie
Penin, François
Pécheur, Eve-Isabelle
author_facet Teissier, Elodie
Penin, François
Pécheur, Eve-Isabelle
author_sort Teissier, Elodie
collection PubMed
description The entry of enveloped viruses into their host cells involves several successive steps, each one being amenable to therapeutic intervention. Entry inhibitors act by targeting viral and/or cellular components, through either the inhibition of protein-protein interactions within the viral envelope proteins or between viral proteins and host cell receptors, or through the inhibition of protein-lipid interactions. Interestingly, inhibitors that concentrate into/onto the membrane in order to target a protein involved in the entry process, such as arbidol or peptide inhibitors of the human immunodeficiency virus (HIV), could allow the use of doses compatible with therapeutic requirements. The efficacy of these drugs validates entry as a point of intervention in viral life cycles. Strategies based upon small molecule antiviral agents, peptides, proteins or nucleic acids, would most likely prove efficient in multidrug combinations, in order to inhibit several steps of virus life cycle and prevent disease progression.
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spelling pubmed-62592792018-12-07 Targeting Cell Entry of Enveloped Viruses as an Antiviral Strategy Teissier, Elodie Penin, François Pécheur, Eve-Isabelle Molecules Review The entry of enveloped viruses into their host cells involves several successive steps, each one being amenable to therapeutic intervention. Entry inhibitors act by targeting viral and/or cellular components, through either the inhibition of protein-protein interactions within the viral envelope proteins or between viral proteins and host cell receptors, or through the inhibition of protein-lipid interactions. Interestingly, inhibitors that concentrate into/onto the membrane in order to target a protein involved in the entry process, such as arbidol or peptide inhibitors of the human immunodeficiency virus (HIV), could allow the use of doses compatible with therapeutic requirements. The efficacy of these drugs validates entry as a point of intervention in viral life cycles. Strategies based upon small molecule antiviral agents, peptides, proteins or nucleic acids, would most likely prove efficient in multidrug combinations, in order to inhibit several steps of virus life cycle and prevent disease progression. MDPI 2010-12-30 /pmc/articles/PMC6259279/ /pubmed/21193846 http://dx.doi.org/10.3390/molecules16010221 Text en © 2010 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Review
Teissier, Elodie
Penin, François
Pécheur, Eve-Isabelle
Targeting Cell Entry of Enveloped Viruses as an Antiviral Strategy
title Targeting Cell Entry of Enveloped Viruses as an Antiviral Strategy
title_full Targeting Cell Entry of Enveloped Viruses as an Antiviral Strategy
title_fullStr Targeting Cell Entry of Enveloped Viruses as an Antiviral Strategy
title_full_unstemmed Targeting Cell Entry of Enveloped Viruses as an Antiviral Strategy
title_short Targeting Cell Entry of Enveloped Viruses as an Antiviral Strategy
title_sort targeting cell entry of enveloped viruses as an antiviral strategy
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6259279/
https://www.ncbi.nlm.nih.gov/pubmed/21193846
http://dx.doi.org/10.3390/molecules16010221
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